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You searched for subject:(adenovirus). Showing records 1 – 30 of 407 total matches.

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Wake Forest University

1. Murrah, Kyle Allen. Viral and Bacterial Polymicrobial Interactions with Streptococcus pneumoniae in Otitis Media.

Degree: 2014, Wake Forest University

 The major pediatric disease otitis media is caused by a variety of bacterial and viral etiological agents, which frequently act in combination to induce polymicrobial… (more)

Subjects/Keywords: Adenovirus

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APA (6th Edition):

Murrah, K. A. (2014). Viral and Bacterial Polymicrobial Interactions with Streptococcus pneumoniae in Otitis Media. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/39396

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Murrah, Kyle Allen. “Viral and Bacterial Polymicrobial Interactions with Streptococcus pneumoniae in Otitis Media.” 2014. Thesis, Wake Forest University. Accessed September 26, 2020. http://hdl.handle.net/10339/39396.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Murrah, Kyle Allen. “Viral and Bacterial Polymicrobial Interactions with Streptococcus pneumoniae in Otitis Media.” 2014. Web. 26 Sep 2020.

Vancouver:

Murrah KA. Viral and Bacterial Polymicrobial Interactions with Streptococcus pneumoniae in Otitis Media. [Internet] [Thesis]. Wake Forest University; 2014. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10339/39396.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Murrah KA. Viral and Bacterial Polymicrobial Interactions with Streptococcus pneumoniae in Otitis Media. [Thesis]. Wake Forest University; 2014. Available from: http://hdl.handle.net/10339/39396

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Wake Forest University

2. Gagliano, Jason. RIBOSOME PROFILING OF LATE ADENOVIRUS INFECTED CELLS REVEALS RIBOSOME STACKING ON THE 5’ UNTRANSLATED REGION OF LATE MESSENGER RNA.

Degree: 2019, Wake Forest University

Adenovirus type 5 is a non-enveloped, icosahedral capsid, containing a linear genome thirty-five thousand base-pairs in length. The genome has 16 genes that, through alternative… (more)

Subjects/Keywords: adenovirus

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APA (6th Edition):

Gagliano, J. (2019). RIBOSOME PROFILING OF LATE ADENOVIRUS INFECTED CELLS REVEALS RIBOSOME STACKING ON THE 5’ UNTRANSLATED REGION OF LATE MESSENGER RNA. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/94309

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Gagliano, Jason. “RIBOSOME PROFILING OF LATE ADENOVIRUS INFECTED CELLS REVEALS RIBOSOME STACKING ON THE 5’ UNTRANSLATED REGION OF LATE MESSENGER RNA.” 2019. Thesis, Wake Forest University. Accessed September 26, 2020. http://hdl.handle.net/10339/94309.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Gagliano, Jason. “RIBOSOME PROFILING OF LATE ADENOVIRUS INFECTED CELLS REVEALS RIBOSOME STACKING ON THE 5’ UNTRANSLATED REGION OF LATE MESSENGER RNA.” 2019. Web. 26 Sep 2020.

Vancouver:

Gagliano J. RIBOSOME PROFILING OF LATE ADENOVIRUS INFECTED CELLS REVEALS RIBOSOME STACKING ON THE 5’ UNTRANSLATED REGION OF LATE MESSENGER RNA. [Internet] [Thesis]. Wake Forest University; 2019. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10339/94309.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gagliano J. RIBOSOME PROFILING OF LATE ADENOVIRUS INFECTED CELLS REVEALS RIBOSOME STACKING ON THE 5’ UNTRANSLATED REGION OF LATE MESSENGER RNA. [Thesis]. Wake Forest University; 2019. Available from: http://hdl.handle.net/10339/94309

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Ottawa

3. McFall, Emily. Exploring Novel Methods to Achieve Systemic Delivery of SMN for Treatment of Spinal Muscular Atrophy .

Degree: 2014, University of Ottawa

 Spinal muscular atrophy (SMA) is an inherited neurodegenerative disease caused by insufficient levels of the survival motor neuron protein (SMN), leading to progressive deterioration of… (more)

Subjects/Keywords: Adenovirus

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APA (6th Edition):

McFall, E. (2014). Exploring Novel Methods to Achieve Systemic Delivery of SMN for Treatment of Spinal Muscular Atrophy . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/31803

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

McFall, Emily. “Exploring Novel Methods to Achieve Systemic Delivery of SMN for Treatment of Spinal Muscular Atrophy .” 2014. Thesis, University of Ottawa. Accessed September 26, 2020. http://hdl.handle.net/10393/31803.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

McFall, Emily. “Exploring Novel Methods to Achieve Systemic Delivery of SMN for Treatment of Spinal Muscular Atrophy .” 2014. Web. 26 Sep 2020.

Vancouver:

McFall E. Exploring Novel Methods to Achieve Systemic Delivery of SMN for Treatment of Spinal Muscular Atrophy . [Internet] [Thesis]. University of Ottawa; 2014. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10393/31803.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

McFall E. Exploring Novel Methods to Achieve Systemic Delivery of SMN for Treatment of Spinal Muscular Atrophy . [Thesis]. University of Ottawa; 2014. Available from: http://hdl.handle.net/10393/31803

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Manitoba

4. Olanubi, Oladunni. Exploitation of human RuvBL1 by HAdV E1A to inhibit interferon response for efficient viral growth.

Degree: Microbiology, 2016, University of Manitoba

 E1A of human adenovirus is the first gene product expressed during viral infection and serves as a preliminary step for efficient viral replication. Other early… (more)

Subjects/Keywords: Adenovirus

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APA (6th Edition):

Olanubi, O. (2016). Exploitation of human RuvBL1 by HAdV E1A to inhibit interferon response for efficient viral growth. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/31993

Chicago Manual of Style (16th Edition):

Olanubi, Oladunni. “Exploitation of human RuvBL1 by HAdV E1A to inhibit interferon response for efficient viral growth.” 2016. Masters Thesis, University of Manitoba. Accessed September 26, 2020. http://hdl.handle.net/1993/31993.

MLA Handbook (7th Edition):

Olanubi, Oladunni. “Exploitation of human RuvBL1 by HAdV E1A to inhibit interferon response for efficient viral growth.” 2016. Web. 26 Sep 2020.

Vancouver:

Olanubi O. Exploitation of human RuvBL1 by HAdV E1A to inhibit interferon response for efficient viral growth. [Internet] [Masters thesis]. University of Manitoba; 2016. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/1993/31993.

Council of Science Editors:

Olanubi O. Exploitation of human RuvBL1 by HAdV E1A to inhibit interferon response for efficient viral growth. [Masters Thesis]. University of Manitoba; 2016. Available from: http://hdl.handle.net/1993/31993

5. Graves, Jason T. THE USE OF REPLICATION-DEFECTIVE ADENOVIRAL VECTORS FOR EXPRESSION OF PRIMORDIAL ATHEROGENIC LIPOPROTEINS IN MICE.

Degree: 2011, Wake Forest University

 The plasma concentration of apolipoprotein B (apoB)-containing lipoproteins is positively associated with several diseases, including atherosclerosis, type 2 diabetes and obesity. Hence, apoB may be… (more)

Subjects/Keywords: adenovirus

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APA (6th Edition):

Graves, J. T. (2011). THE USE OF REPLICATION-DEFECTIVE ADENOVIRAL VECTORS FOR EXPRESSION OF PRIMORDIAL ATHEROGENIC LIPOPROTEINS IN MICE. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/36423

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Graves, Jason T. “THE USE OF REPLICATION-DEFECTIVE ADENOVIRAL VECTORS FOR EXPRESSION OF PRIMORDIAL ATHEROGENIC LIPOPROTEINS IN MICE.” 2011. Thesis, Wake Forest University. Accessed September 26, 2020. http://hdl.handle.net/10339/36423.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Graves, Jason T. “THE USE OF REPLICATION-DEFECTIVE ADENOVIRAL VECTORS FOR EXPRESSION OF PRIMORDIAL ATHEROGENIC LIPOPROTEINS IN MICE.” 2011. Web. 26 Sep 2020.

Vancouver:

Graves JT. THE USE OF REPLICATION-DEFECTIVE ADENOVIRAL VECTORS FOR EXPRESSION OF PRIMORDIAL ATHEROGENIC LIPOPROTEINS IN MICE. [Internet] [Thesis]. Wake Forest University; 2011. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10339/36423.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Graves JT. THE USE OF REPLICATION-DEFECTIVE ADENOVIRAL VECTORS FOR EXPRESSION OF PRIMORDIAL ATHEROGENIC LIPOPROTEINS IN MICE. [Thesis]. Wake Forest University; 2011. Available from: http://hdl.handle.net/10339/36423

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

6. Turner, Roberta Lynn. E1B and E4 adenoviral oncoproteins modulate cellular responses to DNA damage.

Degree: 2013, Wake Forest University

 A productive adenovirus infection inundates the host cell with linear, double-stranded DNA molecules and an abundance of single-stranded DNA. The cellular responses of cell death… (more)

Subjects/Keywords: Adenovirus

…69 Figure 11. PARP-1 is active in adenovirus-infected cells… …83 Figure 15. Cells infected with wild-type adenovirus show increased vesicle formation… …ABBREVIATIONS AAV adeno-associated virus ADP adenovirus death protein Ad adenovirus Adv… …adenovirus AF488 Alexa Fluor 488 AF568 Alexa Fluor 568 AIF apoptosis inducing factor APC/C… …bovine serum albumin CAR coxsackie virus and adenovirus receptor Cdk1 cyclin-dependent… 

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APA (6th Edition):

Turner, R. L. (2013). E1B and E4 adenoviral oncoproteins modulate cellular responses to DNA damage. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/39131

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Turner, Roberta Lynn. “E1B and E4 adenoviral oncoproteins modulate cellular responses to DNA damage.” 2013. Thesis, Wake Forest University. Accessed September 26, 2020. http://hdl.handle.net/10339/39131.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Turner, Roberta Lynn. “E1B and E4 adenoviral oncoproteins modulate cellular responses to DNA damage.” 2013. Web. 26 Sep 2020.

Vancouver:

Turner RL. E1B and E4 adenoviral oncoproteins modulate cellular responses to DNA damage. [Internet] [Thesis]. Wake Forest University; 2013. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10339/39131.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Turner RL. E1B and E4 adenoviral oncoproteins modulate cellular responses to DNA damage. [Thesis]. Wake Forest University; 2013. Available from: http://hdl.handle.net/10339/39131

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

7. Bravo Araya, Maria 1986-. Transduction of Bovine Peripheral Blood Mononuclear Cells with Recombinant Bovine Adenovirus-3 Expressing Chimeric pIX.

Degree: 2018, University of Saskatchewan

 BAdV-3, like many other members of the family Adenoviridae, has been developed and evaluated as a vaccine delivery vehicle in cattle (Ayalew et al., 2014).… (more)

Subjects/Keywords: Bovine adenovirus; tropism; adenovirus vector; PBMCs; pIX

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APA (6th Edition):

Bravo Araya, M. 1. (2018). Transduction of Bovine Peripheral Blood Mononuclear Cells with Recombinant Bovine Adenovirus-3 Expressing Chimeric pIX. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/11669

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Bravo Araya, Maria 1986-. “Transduction of Bovine Peripheral Blood Mononuclear Cells with Recombinant Bovine Adenovirus-3 Expressing Chimeric pIX.” 2018. Thesis, University of Saskatchewan. Accessed September 26, 2020. http://hdl.handle.net/10388/11669.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Bravo Araya, Maria 1986-. “Transduction of Bovine Peripheral Blood Mononuclear Cells with Recombinant Bovine Adenovirus-3 Expressing Chimeric pIX.” 2018. Web. 26 Sep 2020.

Vancouver:

Bravo Araya M1. Transduction of Bovine Peripheral Blood Mononuclear Cells with Recombinant Bovine Adenovirus-3 Expressing Chimeric pIX. [Internet] [Thesis]. University of Saskatchewan; 2018. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10388/11669.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bravo Araya M1. Transduction of Bovine Peripheral Blood Mononuclear Cells with Recombinant Bovine Adenovirus-3 Expressing Chimeric pIX. [Thesis]. University of Saskatchewan; 2018. Available from: http://hdl.handle.net/10388/11669

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

8. Woldemariam, Tekeleselassie Ayalew. Molecular Characterization of Bovine Adenovirus-3 IVa2 Protein.

Degree: 2020, University of Saskatchewan

 ABSTRACT Adenovirus is a naked icosahedral viral particle enclosing a double stranded DNA genome. Adenoviral genes are classified as early, intermediate and late based on… (more)

Subjects/Keywords: Bovine adenovirus IVa2

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APA (6th Edition):

Woldemariam, T. A. (2020). Molecular Characterization of Bovine Adenovirus-3 IVa2 Protein. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12855

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Woldemariam, Tekeleselassie Ayalew. “Molecular Characterization of Bovine Adenovirus-3 IVa2 Protein.” 2020. Thesis, University of Saskatchewan. Accessed September 26, 2020. http://hdl.handle.net/10388/12855.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Woldemariam, Tekeleselassie Ayalew. “Molecular Characterization of Bovine Adenovirus-3 IVa2 Protein.” 2020. Web. 26 Sep 2020.

Vancouver:

Woldemariam TA. Molecular Characterization of Bovine Adenovirus-3 IVa2 Protein. [Internet] [Thesis]. University of Saskatchewan; 2020. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10388/12855.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Woldemariam TA. Molecular Characterization of Bovine Adenovirus-3 IVa2 Protein. [Thesis]. University of Saskatchewan; 2020. Available from: http://hdl.handle.net/10388/12855

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Guelph

9. DENG, LI. Oral inoculation of chickens with a candidate fowl adenovirus 9 vector and functional studies of fowl adenovirus 9 ORF1.

Degree: PhD, Department of Pathobiology, 2015, University of Guelph

 FAdV-9Δ4, lacking six open reading frames (ORFs) 0, 1, 1A, 1B, 1C and 2 at the left end of FAdV-9 genome, shows potential as a… (more)

Subjects/Keywords: fowl adenovirus; dUTPase

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APA (6th Edition):

DENG, L. (2015). Oral inoculation of chickens with a candidate fowl adenovirus 9 vector and functional studies of fowl adenovirus 9 ORF1. (Doctoral Dissertation). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8872

Chicago Manual of Style (16th Edition):

DENG, LI. “Oral inoculation of chickens with a candidate fowl adenovirus 9 vector and functional studies of fowl adenovirus 9 ORF1.” 2015. Doctoral Dissertation, University of Guelph. Accessed September 26, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8872.

MLA Handbook (7th Edition):

DENG, LI. “Oral inoculation of chickens with a candidate fowl adenovirus 9 vector and functional studies of fowl adenovirus 9 ORF1.” 2015. Web. 26 Sep 2020.

Vancouver:

DENG L. Oral inoculation of chickens with a candidate fowl adenovirus 9 vector and functional studies of fowl adenovirus 9 ORF1. [Internet] [Doctoral dissertation]. University of Guelph; 2015. [cited 2020 Sep 26]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8872.

Council of Science Editors:

DENG L. Oral inoculation of chickens with a candidate fowl adenovirus 9 vector and functional studies of fowl adenovirus 9 ORF1. [Doctoral Dissertation]. University of Guelph; 2015. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8872


University of Ottawa

10. Wong, Carmen Man. Improving Adenovirus Efficacy with p14 Fusion Associated Small Transmembrane Protein Expression for Cancer Treatment .

Degree: 2015, University of Ottawa

Adenovirus (Ad) has been one of the most commonly used vectors in gene therapy for many years. One of the limitations of using Ad for… (more)

Subjects/Keywords: Cancer; Adenovirus; Fusion

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APA (6th Edition):

Wong, C. M. (2015). Improving Adenovirus Efficacy with p14 Fusion Associated Small Transmembrane Protein Expression for Cancer Treatment . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/32319

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wong, Carmen Man. “Improving Adenovirus Efficacy with p14 Fusion Associated Small Transmembrane Protein Expression for Cancer Treatment .” 2015. Thesis, University of Ottawa. Accessed September 26, 2020. http://hdl.handle.net/10393/32319.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wong, Carmen Man. “Improving Adenovirus Efficacy with p14 Fusion Associated Small Transmembrane Protein Expression for Cancer Treatment .” 2015. Web. 26 Sep 2020.

Vancouver:

Wong CM. Improving Adenovirus Efficacy with p14 Fusion Associated Small Transmembrane Protein Expression for Cancer Treatment . [Internet] [Thesis]. University of Ottawa; 2015. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10393/32319.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wong CM. Improving Adenovirus Efficacy with p14 Fusion Associated Small Transmembrane Protein Expression for Cancer Treatment . [Thesis]. University of Ottawa; 2015. Available from: http://hdl.handle.net/10393/32319

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Manchester

11. Alissa Alkhalaf, Moustafa. Molecular analysis of adenoviruses from clinical samples.

Degree: PhD, 2011, University of Manchester

 At present, 56 types of human adenovirus (HAdVs) have been identified and found to be associated with a variety of clinical features in the respiratory… (more)

Subjects/Keywords: 616.9; human adenovirus

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APA (6th Edition):

Alissa Alkhalaf, M. (2011). Molecular analysis of adenoviruses from clinical samples. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/molecular-analysis-of-adenoviruses-from-clinical-samples(4b2e8cca-da89-4c8f-a4cc-8dffc489fa49).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.548654

Chicago Manual of Style (16th Edition):

Alissa Alkhalaf, Moustafa. “Molecular analysis of adenoviruses from clinical samples.” 2011. Doctoral Dissertation, University of Manchester. Accessed September 26, 2020. https://www.research.manchester.ac.uk/portal/en/theses/molecular-analysis-of-adenoviruses-from-clinical-samples(4b2e8cca-da89-4c8f-a4cc-8dffc489fa49).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.548654.

MLA Handbook (7th Edition):

Alissa Alkhalaf, Moustafa. “Molecular analysis of adenoviruses from clinical samples.” 2011. Web. 26 Sep 2020.

Vancouver:

Alissa Alkhalaf M. Molecular analysis of adenoviruses from clinical samples. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2020 Sep 26]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/molecular-analysis-of-adenoviruses-from-clinical-samples(4b2e8cca-da89-4c8f-a4cc-8dffc489fa49).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.548654.

Council of Science Editors:

Alissa Alkhalaf M. Molecular analysis of adenoviruses from clinical samples. [Doctoral Dissertation]. University of Manchester; 2011. Available from: https://www.research.manchester.ac.uk/portal/en/theses/molecular-analysis-of-adenoviruses-from-clinical-samples(4b2e8cca-da89-4c8f-a4cc-8dffc489fa49).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.548654


Loyola University Chicago

12. Figueroa, Iris Teresa. The Role of Pidd Protein in Adenoviral Induction of Apoptosis.

Degree: MS, Microbiology and Immunology, 2015, Loyola University Chicago

  The Adenovirus E1A gene sensitizes cells to genetic insults and apoptosis, most notably in response to cytotoxic factors from innate immune cells. The mechanisms… (more)

Subjects/Keywords: Adenovirus; Apoptosis; Virology

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APA (6th Edition):

Figueroa, I. T. (2015). The Role of Pidd Protein in Adenoviral Induction of Apoptosis. (Thesis). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_theses/3132

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Figueroa, Iris Teresa. “The Role of Pidd Protein in Adenoviral Induction of Apoptosis.” 2015. Thesis, Loyola University Chicago. Accessed September 26, 2020. https://ecommons.luc.edu/luc_theses/3132.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Figueroa, Iris Teresa. “The Role of Pidd Protein in Adenoviral Induction of Apoptosis.” 2015. Web. 26 Sep 2020.

Vancouver:

Figueroa IT. The Role of Pidd Protein in Adenoviral Induction of Apoptosis. [Internet] [Thesis]. Loyola University Chicago; 2015. [cited 2020 Sep 26]. Available from: https://ecommons.luc.edu/luc_theses/3132.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Figueroa IT. The Role of Pidd Protein in Adenoviral Induction of Apoptosis. [Thesis]. Loyola University Chicago; 2015. Available from: https://ecommons.luc.edu/luc_theses/3132

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of California – San Diego

13. Miyake-Stoner, Shigeki Joseph. Engineering tumor-specific oncolytic adenoviruses with small molecule-controlled expanded tropisms.

Degree: Biology, 2016, University of California – San Diego

 A promising new strategy for cancer therapy is the use of engineered oncolytic viruses, adapted from their natural properties of seeking out and destroying cells… (more)

Subjects/Keywords: Biology; Adenovirus; Cancer; Oncolytic; Synthetic

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APA (6th Edition):

Miyake-Stoner, S. J. (2016). Engineering tumor-specific oncolytic adenoviruses with small molecule-controlled expanded tropisms. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/7qg226zn

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Miyake-Stoner, Shigeki Joseph. “Engineering tumor-specific oncolytic adenoviruses with small molecule-controlled expanded tropisms.” 2016. Thesis, University of California – San Diego. Accessed September 26, 2020. http://www.escholarship.org/uc/item/7qg226zn.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Miyake-Stoner, Shigeki Joseph. “Engineering tumor-specific oncolytic adenoviruses with small molecule-controlled expanded tropisms.” 2016. Web. 26 Sep 2020.

Vancouver:

Miyake-Stoner SJ. Engineering tumor-specific oncolytic adenoviruses with small molecule-controlled expanded tropisms. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2020 Sep 26]. Available from: http://www.escholarship.org/uc/item/7qg226zn.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Miyake-Stoner SJ. Engineering tumor-specific oncolytic adenoviruses with small molecule-controlled expanded tropisms. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/7qg226zn

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of California – San Diego

14. Partlo, William. Engineered Adenovirus for Selective Replication in Tumors and Druggable Control of Virus Progression.

Degree: Biology, 2018, University of California – San Diego

 The oncolytic Adenovirus has shown promise as a cancer treatment and is under development in numerous laboratories. Two important requirements of an oncolytic Adenovirus are… (more)

Subjects/Keywords: Molecular biology; Adenovirus; Oncolytic

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APA (6th Edition):

Partlo, W. (2018). Engineered Adenovirus for Selective Replication in Tumors and Druggable Control of Virus Progression. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/2k3957sr

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Partlo, William. “Engineered Adenovirus for Selective Replication in Tumors and Druggable Control of Virus Progression.” 2018. Thesis, University of California – San Diego. Accessed September 26, 2020. http://www.escholarship.org/uc/item/2k3957sr.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Partlo, William. “Engineered Adenovirus for Selective Replication in Tumors and Druggable Control of Virus Progression.” 2018. Web. 26 Sep 2020.

Vancouver:

Partlo W. Engineered Adenovirus for Selective Replication in Tumors and Druggable Control of Virus Progression. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2020 Sep 26]. Available from: http://www.escholarship.org/uc/item/2k3957sr.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Partlo W. Engineered Adenovirus for Selective Replication in Tumors and Druggable Control of Virus Progression. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/2k3957sr

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Illinois – Urbana-Champaign

15. Vazquez Bravo, Bernardo. Inactivation mechanisms of adenovirus from exposure to polychromatic ultraviolet light irradiation.

Degree: PhD, Environ Engr in Civil Engr, 2018, University of Illinois – Urbana-Champaign

 Ultraviolet (UV) light is a drinking water treatment technology that has gained popularity as an alternative to control chlorine-resistant pathogens and comply with regulations on… (more)

Subjects/Keywords: Adenovirus; Ultraviolet Light; Inactivation Mechanisms

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APA (6th Edition):

Vazquez Bravo, B. (2018). Inactivation mechanisms of adenovirus from exposure to polychromatic ultraviolet light irradiation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/101327

Chicago Manual of Style (16th Edition):

Vazquez Bravo, Bernardo. “Inactivation mechanisms of adenovirus from exposure to polychromatic ultraviolet light irradiation.” 2018. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 26, 2020. http://hdl.handle.net/2142/101327.

MLA Handbook (7th Edition):

Vazquez Bravo, Bernardo. “Inactivation mechanisms of adenovirus from exposure to polychromatic ultraviolet light irradiation.” 2018. Web. 26 Sep 2020.

Vancouver:

Vazquez Bravo B. Inactivation mechanisms of adenovirus from exposure to polychromatic ultraviolet light irradiation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2018. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/2142/101327.

Council of Science Editors:

Vazquez Bravo B. Inactivation mechanisms of adenovirus from exposure to polychromatic ultraviolet light irradiation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2018. Available from: http://hdl.handle.net/2142/101327


Youngstown State University

16. Zapka, Carrie A. Development of a Rapid Fluorescence-Based Adenovirus Inactivation Assay.

Degree: MSin Chemistry, Department of Chemistry, 2007, Youngstown State University

 Screening of potential antiviral product prototypes is typically performed using The American Society for Testing and Materials (ASTM) method E1052 “Efficacy of Antimicrobial Agents against… (more)

Subjects/Keywords: adenovirus; GFP; time-kill; antiviral

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APA (6th Edition):

Zapka, C. A. (2007). Development of a Rapid Fluorescence-Based Adenovirus Inactivation Assay. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1198694566

Chicago Manual of Style (16th Edition):

Zapka, Carrie A. “Development of a Rapid Fluorescence-Based Adenovirus Inactivation Assay.” 2007. Masters Thesis, Youngstown State University. Accessed September 26, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1198694566.

MLA Handbook (7th Edition):

Zapka, Carrie A. “Development of a Rapid Fluorescence-Based Adenovirus Inactivation Assay.” 2007. Web. 26 Sep 2020.

Vancouver:

Zapka CA. Development of a Rapid Fluorescence-Based Adenovirus Inactivation Assay. [Internet] [Masters thesis]. Youngstown State University; 2007. [cited 2020 Sep 26]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1198694566.

Council of Science Editors:

Zapka CA. Development of a Rapid Fluorescence-Based Adenovirus Inactivation Assay. [Masters Thesis]. Youngstown State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1198694566


University of Adelaide

17. Jagdale, Harshwardhan. Strategies for the development of recombinant porcine adenovirus-based vaccines against Hepatitis C virus.

Degree: 2016, University of Adelaide

 Hepatitis C virus (HCV) infects over 200 million people worldwide and results in persistent infection of approximately 80% of cases. Consequently, HCV is a leading… (more)

Subjects/Keywords: Hepatitis C; adenovirus; vaccine

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APA (6th Edition):

Jagdale, H. (2016). Strategies for the development of recombinant porcine adenovirus-based vaccines against Hepatitis C virus. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/112856

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Jagdale, Harshwardhan. “Strategies for the development of recombinant porcine adenovirus-based vaccines against Hepatitis C virus.” 2016. Thesis, University of Adelaide. Accessed September 26, 2020. http://hdl.handle.net/2440/112856.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Jagdale, Harshwardhan. “Strategies for the development of recombinant porcine adenovirus-based vaccines against Hepatitis C virus.” 2016. Web. 26 Sep 2020.

Vancouver:

Jagdale H. Strategies for the development of recombinant porcine adenovirus-based vaccines against Hepatitis C virus. [Internet] [Thesis]. University of Adelaide; 2016. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/2440/112856.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Jagdale H. Strategies for the development of recombinant porcine adenovirus-based vaccines against Hepatitis C virus. [Thesis]. University of Adelaide; 2016. Available from: http://hdl.handle.net/2440/112856

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Manitoba

18. Frost, Jasmine. Analyzing the interaction of human adenovirus E1A oncoprotein with the cellular proteins Ku70 and FUBP1.

Degree: Microbiology, 2017, University of Manitoba

 Early region 1A proteins (E1A) are the first proteins expressed upon viral infection. E1A is therefore responsible for the remodeling of the intracellular environment to… (more)

Subjects/Keywords: Adenovirus; E1A; Ku70; FUBP1

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APA (6th Edition):

Frost, J. (2017). Analyzing the interaction of human adenovirus E1A oncoprotein with the cellular proteins Ku70 and FUBP1. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/32174

Chicago Manual of Style (16th Edition):

Frost, Jasmine. “Analyzing the interaction of human adenovirus E1A oncoprotein with the cellular proteins Ku70 and FUBP1.” 2017. Masters Thesis, University of Manitoba. Accessed September 26, 2020. http://hdl.handle.net/1993/32174.

MLA Handbook (7th Edition):

Frost, Jasmine. “Analyzing the interaction of human adenovirus E1A oncoprotein with the cellular proteins Ku70 and FUBP1.” 2017. Web. 26 Sep 2020.

Vancouver:

Frost J. Analyzing the interaction of human adenovirus E1A oncoprotein with the cellular proteins Ku70 and FUBP1. [Internet] [Masters thesis]. University of Manitoba; 2017. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/1993/32174.

Council of Science Editors:

Frost J. Analyzing the interaction of human adenovirus E1A oncoprotein with the cellular proteins Ku70 and FUBP1. [Masters Thesis]. University of Manitoba; 2017. Available from: http://hdl.handle.net/1993/32174


Princeton University

19. DeHart, Caroline. Extensive Post-Translational Modification of Endogenous Human p53 .

Degree: PhD, 2013, Princeton University

 The p53 tumor suppressor protein is a central component of numerous cellular signaling pathways and frequently mutated in human cancers. p53 undergoes extensive post-translational modification… (more)

Subjects/Keywords: Adenovirus; Mass spectrometry; p53; PTM

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APA (6th Edition):

DeHart, C. (2013). Extensive Post-Translational Modification of Endogenous Human p53 . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01bv73c053r

Chicago Manual of Style (16th Edition):

DeHart, Caroline. “Extensive Post-Translational Modification of Endogenous Human p53 .” 2013. Doctoral Dissertation, Princeton University. Accessed September 26, 2020. http://arks.princeton.edu/ark:/88435/dsp01bv73c053r.

MLA Handbook (7th Edition):

DeHart, Caroline. “Extensive Post-Translational Modification of Endogenous Human p53 .” 2013. Web. 26 Sep 2020.

Vancouver:

DeHart C. Extensive Post-Translational Modification of Endogenous Human p53 . [Internet] [Doctoral dissertation]. Princeton University; 2013. [cited 2020 Sep 26]. Available from: http://arks.princeton.edu/ark:/88435/dsp01bv73c053r.

Council of Science Editors:

DeHart C. Extensive Post-Translational Modification of Endogenous Human p53 . [Doctoral Dissertation]. Princeton University; 2013. Available from: http://arks.princeton.edu/ark:/88435/dsp01bv73c053r


University College Cork

20. Rajendran, Simon. Ex vivo culture of patient tissue and examination of gene delivery.

Degree: 2014, University College Cork

 Gene therapy has emerged as a realistic prospect for the treatment of cancer due to its potential for selective tumour cell targeting. The greatest challenge… (more)

Subjects/Keywords: Gene delivery; Cancer; Adenovirus

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APA (6th Edition):

Rajendran, S. (2014). Ex vivo culture of patient tissue and examination of gene delivery. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/1904

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Rajendran, Simon. “Ex vivo culture of patient tissue and examination of gene delivery.” 2014. Thesis, University College Cork. Accessed September 26, 2020. http://hdl.handle.net/10468/1904.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Rajendran, Simon. “Ex vivo culture of patient tissue and examination of gene delivery.” 2014. Web. 26 Sep 2020.

Vancouver:

Rajendran S. Ex vivo culture of patient tissue and examination of gene delivery. [Internet] [Thesis]. University College Cork; 2014. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10468/1904.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Rajendran S. Ex vivo culture of patient tissue and examination of gene delivery. [Thesis]. University College Cork; 2014. Available from: http://hdl.handle.net/10468/1904

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of New Mexico

21. Dickson, Laura. Molecular dynamics of adenovirus type 3 and 7 infections in military and civilian populations in the United States.

Degree: Biomedical Sciences Graduate Program, 2009, University of New Mexico

 Human adenoviruses (HAdV) are major causative agents of acute respiratory disease (ARD) worldwide. Military recruits and children are two of the populations most susceptible to… (more)

Subjects/Keywords: Adenovirus; Epidemiology

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APA (6th Edition):

Dickson, L. (2009). Molecular dynamics of adenovirus type 3 and 7 infections in military and civilian populations in the United States. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/42

Chicago Manual of Style (16th Edition):

Dickson, Laura. “Molecular dynamics of adenovirus type 3 and 7 infections in military and civilian populations in the United States.” 2009. Masters Thesis, University of New Mexico. Accessed September 26, 2020. https://digitalrepository.unm.edu/biom_etds/42.

MLA Handbook (7th Edition):

Dickson, Laura. “Molecular dynamics of adenovirus type 3 and 7 infections in military and civilian populations in the United States.” 2009. Web. 26 Sep 2020.

Vancouver:

Dickson L. Molecular dynamics of adenovirus type 3 and 7 infections in military and civilian populations in the United States. [Internet] [Masters thesis]. University of New Mexico; 2009. [cited 2020 Sep 26]. Available from: https://digitalrepository.unm.edu/biom_etds/42.

Council of Science Editors:

Dickson L. Molecular dynamics of adenovirus type 3 and 7 infections in military and civilian populations in the United States. [Masters Thesis]. University of New Mexico; 2009. Available from: https://digitalrepository.unm.edu/biom_etds/42


Georgia State University

22. Murali, Vineeth Kumar. Adenovirus Death Protein: The Switch Between Lytic and Persistent Infections in Lymphocytes?.

Degree: MS, Biology, 2012, Georgia State University

  ABSTRACT Adenovirus Death Protein (ADP) expression during late stages of a lytic infection releases mature virions to promote viral spread, thus leading to death… (more)

Subjects/Keywords: Adenovirus; ADP; Persistent infection; Lymphocytes

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APA (6th Edition):

Murali, V. K. (2012). Adenovirus Death Protein: The Switch Between Lytic and Persistent Infections in Lymphocytes?. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_theses/41

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Murali, Vineeth Kumar. “Adenovirus Death Protein: The Switch Between Lytic and Persistent Infections in Lymphocytes?.” 2012. Thesis, Georgia State University. Accessed September 26, 2020. https://scholarworks.gsu.edu/biology_theses/41.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Murali, Vineeth Kumar. “Adenovirus Death Protein: The Switch Between Lytic and Persistent Infections in Lymphocytes?.” 2012. Web. 26 Sep 2020.

Vancouver:

Murali VK. Adenovirus Death Protein: The Switch Between Lytic and Persistent Infections in Lymphocytes?. [Internet] [Thesis]. Georgia State University; 2012. [cited 2020 Sep 26]. Available from: https://scholarworks.gsu.edu/biology_theses/41.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Murali VK. Adenovirus Death Protein: The Switch Between Lytic and Persistent Infections in Lymphocytes?. [Thesis]. Georgia State University; 2012. Available from: https://scholarworks.gsu.edu/biology_theses/41

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Wright State University

23. Kolawole, Abimbola Olayinka. The Molecular Basis of the Interaction Between the Coxsackievirus and Adenovirus Receptor (CAR) and MAGI-1.

Degree: PhD, Biomedical Sciences PhD, 2011, Wright State University

 A major factor in virus entry into cells is localization and abundance of the primary receptor. The Coxsackievirus and adenovirus receptor (CAR) is the primary… (more)

Subjects/Keywords: Biomedical Research; coxsackievirus and adenovirus receptor; CAR; MAGI-1; adenovirus; epithelia

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APA (6th Edition):

Kolawole, A. O. (2011). The Molecular Basis of the Interaction Between the Coxsackievirus and Adenovirus Receptor (CAR) and MAGI-1. (Doctoral Dissertation). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1320947325

Chicago Manual of Style (16th Edition):

Kolawole, Abimbola Olayinka. “The Molecular Basis of the Interaction Between the Coxsackievirus and Adenovirus Receptor (CAR) and MAGI-1.” 2011. Doctoral Dissertation, Wright State University. Accessed September 26, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1320947325.

MLA Handbook (7th Edition):

Kolawole, Abimbola Olayinka. “The Molecular Basis of the Interaction Between the Coxsackievirus and Adenovirus Receptor (CAR) and MAGI-1.” 2011. Web. 26 Sep 2020.

Vancouver:

Kolawole AO. The Molecular Basis of the Interaction Between the Coxsackievirus and Adenovirus Receptor (CAR) and MAGI-1. [Internet] [Doctoral dissertation]. Wright State University; 2011. [cited 2020 Sep 26]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1320947325.

Council of Science Editors:

Kolawole AO. The Molecular Basis of the Interaction Between the Coxsackievirus and Adenovirus Receptor (CAR) and MAGI-1. [Doctoral Dissertation]. Wright State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1320947325


University of New Mexico

24. Dowling, James. Progeny Release of Species B Human Adenoviruses Is Not Mediated By Early Region 3 Proteins 20.1K, 20.5k, and 10.9k.

Degree: Biomedical Sciences Graduate Program, 2013, University of New Mexico

 The early region 3 (E3) of the human adenovirus (HAdV) genome encodes proteins that regulate the host immune response to viral infection. The E3 region… (more)

Subjects/Keywords: adenovirus; human adenovirus; early region 3; E3; E3-20.1K; E3-20.5K; E3-10.9K; species b human adenovirus

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APA (6th Edition):

Dowling, J. (2013). Progeny Release of Species B Human Adenoviruses Is Not Mediated By Early Region 3 Proteins 20.1K, 20.5k, and 10.9k. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/69

Chicago Manual of Style (16th Edition):

Dowling, James. “Progeny Release of Species B Human Adenoviruses Is Not Mediated By Early Region 3 Proteins 20.1K, 20.5k, and 10.9k.” 2013. Masters Thesis, University of New Mexico. Accessed September 26, 2020. https://digitalrepository.unm.edu/biom_etds/69.

MLA Handbook (7th Edition):

Dowling, James. “Progeny Release of Species B Human Adenoviruses Is Not Mediated By Early Region 3 Proteins 20.1K, 20.5k, and 10.9k.” 2013. Web. 26 Sep 2020.

Vancouver:

Dowling J. Progeny Release of Species B Human Adenoviruses Is Not Mediated By Early Region 3 Proteins 20.1K, 20.5k, and 10.9k. [Internet] [Masters thesis]. University of New Mexico; 2013. [cited 2020 Sep 26]. Available from: https://digitalrepository.unm.edu/biom_etds/69.

Council of Science Editors:

Dowling J. Progeny Release of Species B Human Adenoviruses Is Not Mediated By Early Region 3 Proteins 20.1K, 20.5k, and 10.9k. [Masters Thesis]. University of New Mexico; 2013. Available from: https://digitalrepository.unm.edu/biom_etds/69

25. 鄭, 朱蒙 パトリック. アデノウイルスの増殖にはARE-mRNAの安定化システムが必要である : ARE-mRNA stabilization system is necessary to replicate adenovirus.

Degree: 博士(歯学), 2016, Hokkaido University / 北海道大学

AU-rich element (ARE)はがん遺伝子など, 主に細胞増殖にかかわる多くの遺伝子の mRNA に含まれている遺伝子領域で, RNA 結合タンパク HUR が AREに特異的に結合することによって ARE-mRNA を核外輸送・安定化することが知られている. アデノウイルスの初期遺伝子タンパク E4orf6 による細胞がん化には, ARE-mRNA の恒常的な核外輸送・安定化が必須であることが解明されている. しかしながら, このシステムとアデノウイルスの増殖にどのような関連が存在するかはいまだ不明である. 本研究ではアデノウイルスが ARE-mRNAとそれに結合する HUR タンパクのウイルス増殖に及ぼす影響について検討した. Tet-off… (more)

Subjects/Keywords: Adenovirus; E4orf6; HUR; ARE-mRNA stability

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APA (6th Edition):

鄭, . . (2016). アデノウイルスの増殖にはARE-mRNAの安定化システムが必要である : ARE-mRNA stabilization system is necessary to replicate adenovirus. (Thesis). Hokkaido University / 北海道大学. Retrieved from http://hdl.handle.net/2115/67917 ; http://dx.doi.org/10.14943/doctoral.k12163

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

鄭, 朱蒙 パトリック. “アデノウイルスの増殖にはARE-mRNAの安定化システムが必要である : ARE-mRNA stabilization system is necessary to replicate adenovirus.” 2016. Thesis, Hokkaido University / 北海道大学. Accessed September 26, 2020. http://hdl.handle.net/2115/67917 ; http://dx.doi.org/10.14943/doctoral.k12163.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

鄭, 朱蒙 パトリック. “アデノウイルスの増殖にはARE-mRNAの安定化システムが必要である : ARE-mRNA stabilization system is necessary to replicate adenovirus.” 2016. Web. 26 Sep 2020.

Vancouver:

鄭 . アデノウイルスの増殖にはARE-mRNAの安定化システムが必要である : ARE-mRNA stabilization system is necessary to replicate adenovirus. [Internet] [Thesis]. Hokkaido University / 北海道大学; 2016. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/2115/67917 ; http://dx.doi.org/10.14943/doctoral.k12163.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

鄭 . アデノウイルスの増殖にはARE-mRNAの安定化システムが必要である : ARE-mRNA stabilization system is necessary to replicate adenovirus. [Thesis]. Hokkaido University / 北海道大学; 2016. Available from: http://hdl.handle.net/2115/67917 ; http://dx.doi.org/10.14943/doctoral.k12163

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Alberta

26. Miklavcic, John. Ganglioside Increases Metastatic Potential and Susceptibility of Prostate Cancer to Gene Therapy in vitro.

Degree: MS, Department of Agricultural, Food and Nutritional Science, 2009, University of Alberta

 Prostate cancer (CaP) is the 2nd most common cancer in North American men. Tumour management strategies are appropriate for early stage disease, but advanced disease… (more)

Subjects/Keywords: adenovirus; gene therapy; metastasis; prostate cancer; ganglioside

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APA (6th Edition):

Miklavcic, J. (2009). Ganglioside Increases Metastatic Potential and Susceptibility of Prostate Cancer to Gene Therapy in vitro. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/m613mx76k

Chicago Manual of Style (16th Edition):

Miklavcic, John. “Ganglioside Increases Metastatic Potential and Susceptibility of Prostate Cancer to Gene Therapy in vitro.” 2009. Masters Thesis, University of Alberta. Accessed September 26, 2020. https://era.library.ualberta.ca/files/m613mx76k.

MLA Handbook (7th Edition):

Miklavcic, John. “Ganglioside Increases Metastatic Potential and Susceptibility of Prostate Cancer to Gene Therapy in vitro.” 2009. Web. 26 Sep 2020.

Vancouver:

Miklavcic J. Ganglioside Increases Metastatic Potential and Susceptibility of Prostate Cancer to Gene Therapy in vitro. [Internet] [Masters thesis]. University of Alberta; 2009. [cited 2020 Sep 26]. Available from: https://era.library.ualberta.ca/files/m613mx76k.

Council of Science Editors:

Miklavcic J. Ganglioside Increases Metastatic Potential and Susceptibility of Prostate Cancer to Gene Therapy in vitro. [Masters Thesis]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/m613mx76k


Loyola University Chicago

27. Marvin, Shauna. Evading Innate and Adaptive Immunity During Adenovirus Cell Entry.

Degree: PhD, Microbiology and Immunology, 2013, Loyola University Chicago

Adenovirus (Ad), a non-enveloped, dsDNA virus, enters cells via clathrin-mediated endocytosis. For viral genome delivery to the nucleus, Ad must penetrate endosomal membranes to… (more)

Subjects/Keywords: Adenovirus; autophagy; galectin; membrane rupture; Virology

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Marvin, S. (2013). Evading Innate and Adaptive Immunity During Adenovirus Cell Entry. (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/533

Chicago Manual of Style (16th Edition):

Marvin, Shauna. “Evading Innate and Adaptive Immunity During Adenovirus Cell Entry.” 2013. Doctoral Dissertation, Loyola University Chicago. Accessed September 26, 2020. https://ecommons.luc.edu/luc_diss/533.

MLA Handbook (7th Edition):

Marvin, Shauna. “Evading Innate and Adaptive Immunity During Adenovirus Cell Entry.” 2013. Web. 26 Sep 2020.

Vancouver:

Marvin S. Evading Innate and Adaptive Immunity During Adenovirus Cell Entry. [Internet] [Doctoral dissertation]. Loyola University Chicago; 2013. [cited 2020 Sep 26]. Available from: https://ecommons.luc.edu/luc_diss/533.

Council of Science Editors:

Marvin S. Evading Innate and Adaptive Immunity During Adenovirus Cell Entry. [Doctoral Dissertation]. Loyola University Chicago; 2013. Available from: https://ecommons.luc.edu/luc_diss/533


North Carolina State University

28. Ventevogel, Melissa Samo. Cytokine Modulation of Thymopoiesis.

Degree: MS, Immunology, 2008, North Carolina State University

 The thymus is an organ derived from embryonic endoderm and mesoderm differentiation. It is located above the heart and is made up of two compartments,… (more)

Subjects/Keywords: cytokine; adenovirus; thymopoiesis

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APA (6th Edition):

Ventevogel, M. S. (2008). Cytokine Modulation of Thymopoiesis. (Thesis). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/2947

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ventevogel, Melissa Samo. “Cytokine Modulation of Thymopoiesis.” 2008. Thesis, North Carolina State University. Accessed September 26, 2020. http://www.lib.ncsu.edu/resolver/1840.16/2947.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ventevogel, Melissa Samo. “Cytokine Modulation of Thymopoiesis.” 2008. Web. 26 Sep 2020.

Vancouver:

Ventevogel MS. Cytokine Modulation of Thymopoiesis. [Internet] [Thesis]. North Carolina State University; 2008. [cited 2020 Sep 26]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/2947.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ventevogel MS. Cytokine Modulation of Thymopoiesis. [Thesis]. North Carolina State University; 2008. Available from: http://www.lib.ncsu.edu/resolver/1840.16/2947

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


North Carolina State University

29. Culver, Carolyn Anne. Adenovirus Triggers Reorganization of Vimentin-Containing Intermediate Filaments Resulting in the Perinuclear Movement of cPLA2 and Suppression of Prostaglandin Production.

Degree: PhD, Microbiology, 2008, North Carolina State University

 ABSTRACT CULVER, CAROLYN ANNE. Adenovirus triggers reorganization of vimentin-containing intermediate filaments resulting in the perinuclear movement of cPLA2 and suppression of prostaglandin production. (Under the… (more)

Subjects/Keywords: cPLA2; vimentin; adenovirus

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APA (6th Edition):

Culver, C. A. (2008). Adenovirus Triggers Reorganization of Vimentin-Containing Intermediate Filaments Resulting in the Perinuclear Movement of cPLA2 and Suppression of Prostaglandin Production. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/5242

Chicago Manual of Style (16th Edition):

Culver, Carolyn Anne. “Adenovirus Triggers Reorganization of Vimentin-Containing Intermediate Filaments Resulting in the Perinuclear Movement of cPLA2 and Suppression of Prostaglandin Production.” 2008. Doctoral Dissertation, North Carolina State University. Accessed September 26, 2020. http://www.lib.ncsu.edu/resolver/1840.16/5242.

MLA Handbook (7th Edition):

Culver, Carolyn Anne. “Adenovirus Triggers Reorganization of Vimentin-Containing Intermediate Filaments Resulting in the Perinuclear Movement of cPLA2 and Suppression of Prostaglandin Production.” 2008. Web. 26 Sep 2020.

Vancouver:

Culver CA. Adenovirus Triggers Reorganization of Vimentin-Containing Intermediate Filaments Resulting in the Perinuclear Movement of cPLA2 and Suppression of Prostaglandin Production. [Internet] [Doctoral dissertation]. North Carolina State University; 2008. [cited 2020 Sep 26]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5242.

Council of Science Editors:

Culver CA. Adenovirus Triggers Reorganization of Vimentin-Containing Intermediate Filaments Resulting in the Perinuclear Movement of cPLA2 and Suppression of Prostaglandin Production. [Doctoral Dissertation]. North Carolina State University; 2008. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5242


University of Toronto

30. Grosso, Filomena Sarina. Cardiotonic Steroids Suppress Adenovirus Replication.

Degree: 2018, University of Toronto

Human adenoviruses are common pathogens that can cause life-threatening illness, yet no approved therapies are available for treatment. This work shows that two cardiotonic steroids,… (more)

Subjects/Keywords: adenovirus; anti-viral therapy; cardiotonic steroids; 0720

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Grosso, F. S. (2018). Cardiotonic Steroids Suppress Adenovirus Replication. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/89539

Chicago Manual of Style (16th Edition):

Grosso, Filomena Sarina. “Cardiotonic Steroids Suppress Adenovirus Replication.” 2018. Masters Thesis, University of Toronto. Accessed September 26, 2020. http://hdl.handle.net/1807/89539.

MLA Handbook (7th Edition):

Grosso, Filomena Sarina. “Cardiotonic Steroids Suppress Adenovirus Replication.” 2018. Web. 26 Sep 2020.

Vancouver:

Grosso FS. Cardiotonic Steroids Suppress Adenovirus Replication. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/1807/89539.

Council of Science Editors:

Grosso FS. Cardiotonic Steroids Suppress Adenovirus Replication. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89539

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